| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057515420 | 1.000 | 0.080 | 7 | 100819874 | missense variant | G/A | snv | 1 | |||
| rs121908601 | 0.851 | 0.080 | 8 | 105419192 | missense variant | A/C;G | snv | 4.0E-06; 2.7E-03 | 4 | ||
| rs187043152 | 0.851 | 0.080 | 8 | 105801714 | missense variant | G/A;T | snv | 3.4E-03; 4.0E-06 | 4 | ||
| rs28374544 | 1.000 | 0.080 | 8 | 105802051 | missense variant | A/G | snv | 1.1E-02 | 4.4E-02 | 1 | |
| rs121908603 | 0.882 | 0.120 | 8 | 105802189 | missense variant | A/C;G | snv | 4.9E-04; 4.0E-06 | 3 | ||
| rs1448468136 | 1.000 | 0.080 | 8 | 105802610 | missense variant | C/A;T | snv | 1 | |||
| rs145895196 | 0.925 | 0.120 | 20 | 10641566 | missense variant | C/A;T | snv | 1.6E-05; 1.9E-03 | 2 | ||
| rs769531968 | 0.925 | 0.120 | 20 | 10643807 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 2 | |
| rs28939668 | 0.807 | 0.200 | 20 | 10652533 | missense variant | C/T | snv | 6 | |||
| rs1131695 | 1.000 | 0.080 | 20 | 10652589 | stop gained | G/A;C;T | snv | 0.46 | 1 | ||
| rs121918351 | 0.882 | 0.240 | 20 | 10658611 | missense variant | C/T | snv | 3 | |||
| rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
| rs653178 | 0.672 | 0.600 | 12 | 111569952 | intron variant | C/T | snv | 0.67 | 41 | ||
| rs11065987 | 0.807 | 0.280 | 12 | 111634620 | intergenic variant | A/G | snv | 0.29 | 17 | ||
| rs17696736 | 0.827 | 0.240 | 12 | 112049014 | intron variant | A/G | snv | 0.30 | 18 | ||
| rs11066188 | 0.851 | 0.320 | 12 | 112172910 | intron variant | G/A;C | snv | 0.30; 4.1E-06 | 7 | ||
| rs11066320 | 0.925 | 0.120 | 12 | 112468611 | intron variant | A/G | snv | 0.70 | 5 | ||
| rs233722 | 1.000 | 0.080 | 12 | 112593670 | intron variant | G/A | snv | 0.53 | 1 | ||
| rs233716 | 1.000 | 0.080 | 12 | 112602139 | intron variant | C/T | snv | 0.58 | 1 | ||
| rs864321699 | 1.000 | 0.080 | 8 | 11708337 | missense variant | G/A;C | snv | 2 | |||
| rs387906769 | 0.807 | 0.080 | 8 | 11708799 | missense variant | C/T | snv | 7.3E-05 | 4.2E-05 | 7 | |
| rs17153694 | 0.851 | 0.160 | 8 | 11730972 | intron variant | C/T | snv | 0.12 | 4 | ||
| rs771792843 | 1.000 | 0.080 | 8 | 11749060 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs804280 | 0.882 | 0.120 | 8 | 11755189 | intron variant | C/A;G | snv | 6 | |||
| rs4841587 | 1.000 | 0.080 | 8 | 11756666 | non coding transcript exon variant | G/T | snv | 0.37 | 3 |